aplasia of the pectoralis major muscle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence of the pectoralis major muscle. (Human Phenotype Ontology, HP_0009751)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009751
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Genes

3 genes associated with the aplasia of the pectoralis major muscle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NSDHL NAD(P) dependent steroid dehydrogenase-like
TBX3 T-box 3
TBX5 T-box 5